A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15184986



Internal ID3530033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24861890..24864325hg38UCSC Ensembl
Innerchr15:24861890..24864325hg38UCSC Ensembl
Outerchr15:24861602..24864594hg38UCSC Ensembl
chr15:25107037..25109472hg19UCSC Ensembl
Innerchr15:25107037..25109472hg19UCSC Ensembl
Outerchr15:25106749..25109741hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382436
hg192436
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635909
Supporting Variants
SamplesHG03123
Known GenesSNRPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15184986
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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